CA2400993A1 - Carriers coated with polysaccharides, their preparation and use - Google Patents
Carriers coated with polysaccharides, their preparation and use Download PDFInfo
- Publication number
- CA2400993A1 CA2400993A1 CA002400993A CA2400993A CA2400993A1 CA 2400993 A1 CA2400993 A1 CA 2400993A1 CA 002400993 A CA002400993 A CA 002400993A CA 2400993 A CA2400993 A CA 2400993A CA 2400993 A1 CA2400993 A1 CA 2400993A1
- Authority
- CA
- Canada
- Prior art keywords
- carrier
- functional groups
- polysaccharide
- layer
- carrier according
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/543—Immunoassay; Biospecific binding assay; Materials therefor with an insoluble carrier for immobilising immunochemicals
- G01N33/544—Immunoassay; Biospecific binding assay; Materials therefor with an insoluble carrier for immobilising immunochemicals the carrier being organic
- G01N33/548—Carbohydrates, e.g. dextran
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S435/00—Chemistry: molecular biology and microbiology
- Y10S435/969—Multiple layering of reactants
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S436/00—Chemistry: analytical and immunological testing
- Y10S436/827—Lectins
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
- Y10T428/2991—Coated
Abstract
A polysaccharide coated carrier having a coating of at least two successive layers of polysaccharide. The first polysaccharide layer spontaneously associates with a second polysaccharide layer and, optionally, the carrier. Each successive layer of polysaccharide spontaneously associates with a preceding layer. Spontaneous association occurs due to the presence of oppositely charged functional groups on each layer of polysaccharide or due to a spontaneous reaction between the functional groups the layers. The carrier may be any surface such as a tube, microtitration plate, bead, particle or t he like and is suitable for use in diagnostic or therapeutic methods.
Claims (39)
1. A polysaccharide coated carrier comprising a carrier having a coating of at least two successive layers of polysaccharides, wherein a first polysaccharide layer spontaneously associates with a second polysaccharide layer.
2. The carrier of claim 1 wherein each of said successive polysaccharide layer spontaneously associates with each of a preceding polysaccharide layer.
3. The carrier of claim 1 wherein said polysaccharides have pendent functional groups and said functional groups of said successive polysaccharide layers are charged oppositely of said functional groups of said preceding polysaccharide layers.
4. The carrier of claim 1 wherein said polysaccharides have pendant functional groups and said successive layers of polysaccharide are covalently coupled to said preceding polysaccharide layers by reaction between said functional groups of said successive layers with said functional groups of said preceding layers.
5. The carrier of claim 4 wherein the reaction between said functional groups is a spontaneous reaction.
6. The carrier according to claim 4 wherein said functional groups of said successive polysaccharide layers alternate between amine functional groups and amine-reactive functional groups.
7. The carrier according to claim 6 wherein the amine reactive functional group is an aldehyde group or a carboxyl group.
8. The carrier of claim 1 wherein said first polysaccharide layer spontaneously associates with said carrier.
9. ~The carrier of claim 8 wherein said carrier and said polysaccharides have pendent functional groups
10. The carrier of claim 9 wherein said functional groups of said carrier and said functional groups of said first polysaccharide layer are the cause of the spontaneous association.
11. The carrier of claim 9 wherein said functional groups of said carrier and said functional groups of said first polysaccharide layer are oppositely charged.
12. The carrier of claim 9 wherein said carrier and said polysaccharides have pendent functional groups, and said first polysaccharide layer is covalently coupled to said carrier by reaction between said functional groups of said carrier and said functional groups of said first polysaccharide layer.
13. The carrier of claim 12 wherein the reaction between said functional groups is a spontaneous reaction.
14. The carrier according to claim 12 wherein said functional groups of said carrier is an amine reactive functional groups and the functional groups of said first polysaccharide layer are amine functional groups.
15. The carrier of claim 14 wherein said amine reactive functional group is an aldehyde group or a carboxyl group.
16. The carrier according to any one of claims 1 through 15 wherein said carrier material is selected from the group consisting of natural, synthetic or modified naturally occurring polymers such as agarose, cellulose, nitrocellulose,~
cellulose acetate, polyvinylchloride, polystyrene, polyethylene, polypropylene,~
poly(4-methylbutene), polyacrylamide, polymethacrylate, polyethyleneterephthalate, nylon, polyvinylbutyrate or polyacrylat; silicones;
glasses; ceramics; inorganic powders such as silica, magnesium sulfate and alumina; magnetic materials; metals; or a combination thereof.
cellulose acetate, polyvinylchloride, polystyrene, polyethylene, polypropylene,~
poly(4-methylbutene), polyacrylamide, polymethacrylate, polyethyleneterephthalate, nylon, polyvinylbutyrate or polyacrylat; silicones;
glasses; ceramics; inorganic powders such as silica, magnesium sulfate and alumina; magnetic materials; metals; or a combination thereof.
17. The carrier according to any one of claims 1 through 16 wherein said carrier is selected from the group consisting of strips, sheets, rods, tubes, wells, microtitration plates, beads and particles.
18. The carrier according to claim 17 wherein said carrier is a magnetic or non-magnetic particle.
19. The carrier according to claim 18 wherein said carrier is a carboxylated latex particle.
20. The carrier according to claim 18 wherein said particle is in the size range of 0.1 to 10 µm, preferably 0.1 to 5 µm, most preferably 0.15 to 3 µm.
21. The carrier according to any one of claims 1 through 20 wherein said carrier is associated with at least one reporter molecule.
22. The carrier according to claim 21 wherein said reporter molecule is selected from the group consisting of dyes, radiolabels, sensitizers, fluorescers and/or chemiluminescers.
23. The carrier according to any one of claims 1 through 22 wherein the polysaccharide of the first coating layer is an aminodextran.
24. The carrier according to claim 23 wherein said aminodextran has a molecular weight of 10,000 to 2,000,000.
25. The carrier according to any of the preceding claims wherein the outermost layer of polysaccharide has at least one pendent functional group.
26. The carrier according to claim 25 wherein said pendent functional group is selected from the group consisting of amines, aldehydes, carboxyl groups, maleimido groups, or sulfhydryl groups.
27. The carrier according to claims 25 or 26 wherein said pendent functional group is bound to a specific binding partner.
28. The carrier according to claim 27 wherein said specific binding partner is selected from the group consisting of antibodies, antibody fragments, receptors, ligands, oligonucleotides, oligonucleotide-binding proteins, lectins, haptens, antigens, immunoglobulin binding proteins, avidin, streptavidin, or biotin.
29. A method for preparing the polysaccharide coated carrier of claim 1 comprising:
(a) covalently coupling the first polysaccharide layer to said carrier by reaction between the amine reactive functional groups of the carrier and the amine functional groups of the polysaccharides of the first coating layer; and (b) covalently coupling the second polysaccharide layer to the first polysaccharide layer by reaction between the amine functional groups of the first polysaccharide layer and the amine reactive functional groups of the second polysaccharide layer.
(a) covalently coupling the first polysaccharide layer to said carrier by reaction between the amine reactive functional groups of the carrier and the amine functional groups of the polysaccharides of the first coating layer; and (b) covalently coupling the second polysaccharide layer to the first polysaccharide layer by reaction between the amine functional groups of the first polysaccharide layer and the amine reactive functional groups of the second polysaccharide layer.
30. A method for preparing the polysaccharide coated carrier of claim 1 comprising:
(a) covalently coupling the first polysaccharide layer to said carrier by reaction between the amine functional groups of the carrier and the amine reactive functional groups of the polysaccharides of the first coating layer; and (b) covalently coupling the second polysaccharide layer to the first polysaccharide layer by reaction between the amine reactive functional groups of the first polysaccharide layer and the amine functional groups of the second polysaccharide layer.
(a) covalently coupling the first polysaccharide layer to said carrier by reaction between the amine functional groups of the carrier and the amine reactive functional groups of the polysaccharides of the first coating layer; and (b) covalently coupling the second polysaccharide layer to the first polysaccharide layer by reaction between the amine reactive functional groups of the first polysaccharide layer and the amine functional groups of the second polysaccharide layer.
31. The method according to claims 29 or 30 wherein carbodiimide conjugation chemistry is used for the coupling of the polysaccharides of the first coating layer to said carrier.
32. The method according to any one of claims 29 through 31 wherein the coupling of the polysaccharides of the second coating layer to the first coating layer is done in the presence of a mild reducing agent, such as sodium cyanoborhydride.
33. The method according to any one of claims 29 through 31 wherein carbodiimide conjugation chemistry is used for the coupling of the polysaccharides of the second coating layer to the first coating layer.
34. The method according to any one of claims 29 through 33 wherein the specific binding partners are covalently bound to the coating layer by reaction between the pendent functional groups of the coating layer and functional groups of the specific binding partners.
35. The carrier according to any one of claims 1 through 28 for use in in-vitro and/or in-vivo diagnostic methods.
36. The carrier according to any one of claims 1 through 28 for use in a method for the quantitative and/or qualitative determination of an analyte.
37. Composition comprising the carrier according to any one of claims 1 through 28 in a pharmaceutically acceptable medium.
38. The carrier according to any one of claims 1 through 28 for use in a therapeutic method.
39. A method for quantitative or qualitative determination of an analyte in a sample using the carrier according to any one of claims 1 through 28.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/US2000/005978 WO2001067105A1 (en) | 2000-03-06 | 2000-03-06 | Carriers coated with polysaccharides, their preparation and use |
Publications (2)
Publication Number | Publication Date |
---|---|
CA2400993A1 true CA2400993A1 (en) | 2001-09-13 |
CA2400993C CA2400993C (en) | 2011-06-07 |
Family
ID=21741129
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA2400993A Expired - Lifetime CA2400993C (en) | 2000-03-06 | 2000-03-06 | Carriers coated with polysaccharides, their preparation and use |
Country Status (7)
Country | Link |
---|---|
US (1) | US7179660B1 (en) |
EP (1) | EP1264181B1 (en) |
JP (1) | JP4448642B2 (en) |
CA (1) | CA2400993C (en) |
DE (1) | DE60035127T2 (en) |
ES (1) | ES2287006T3 (en) |
WO (1) | WO2001067105A1 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113125705A (en) * | 2019-12-31 | 2021-07-16 | 博阳生物科技(上海)有限公司 | Homogeneous detection kit for myoglobin and application thereof |
CN113125703A (en) * | 2019-12-31 | 2021-07-16 | 博阳生物科技(上海)有限公司 | Homogeneous detection kit for myoglobin and application thereof |
Families Citing this family (67)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20020164825A1 (en) * | 2000-09-09 | 2002-11-07 | Wen-Tien Chen | Cell separation matrix |
EP1546723A4 (en) * | 2002-08-16 | 2007-03-07 | Decision Biomarkers Inc | Reading of fluorescent arrays |
DE10318801A1 (en) * | 2003-04-17 | 2004-11-04 | Aesculap Ag & Co. Kg | Flat implant and its use in surgery |
EP1494028A1 (en) * | 2003-07-03 | 2005-01-05 | Labsoft Diagnostics AG | Immunomagnetic separation of specific target cells |
JP4665161B2 (en) * | 2004-02-06 | 2011-04-06 | 国立大学法人高知大学 | Method for measuring Raman spectrum, noble metal particles used in the method, and method for producing the noble metal particles |
CN104090097B (en) * | 2004-02-26 | 2017-04-12 | 康多尔生物技术有限公司 | Aqueous solution of specificity binding interaction culture medium serving as binding pair |
US7887880B2 (en) * | 2004-06-30 | 2011-02-15 | Auburn University | Preparation and application of stabilized iron nanoparticles for dechlorination of chlorinated hydrocarbons in soils, sediments, and ground water |
US20060040258A1 (en) * | 2004-08-23 | 2006-02-23 | Huiyan Guo | Water-soluble conjugates and methods of preparation |
DE102004042124B4 (en) * | 2004-08-30 | 2006-07-06 | Dade Behring Marburg Gmbh | Homogeneous method for the determination of an analyte in the presence of an excess of cross-reacting substances |
CA2595292C (en) * | 2005-01-20 | 2014-03-04 | Luminex Corporation | Magnetic microspheres for use in fluorescence-based applications |
US20060166376A1 (en) * | 2005-01-21 | 2006-07-27 | Craig Alan R | Compositions for use as a signal generation component and methods of using same |
EP1715344A1 (en) * | 2005-04-22 | 2006-10-25 | Universiteit Utrecht Holding B.V. | Immobilisation of antigenic carbohydrates to support detection of pathogenic micro-organisms |
JP2006321932A (en) * | 2005-05-20 | 2006-11-30 | Jsr Corp | Carrier polymer particle and its production method |
JP4873123B2 (en) * | 2005-11-28 | 2012-02-08 | Jsr株式会社 | Method for producing carrier polymer particles |
WO2006123686A1 (en) * | 2005-05-20 | 2006-11-23 | Jsr Corporation | Support polymer particle, process for producing the same, magnetic particle for specific trapping, and process for producing the same |
JP5007920B2 (en) * | 2005-08-31 | 2012-08-22 | 日立金属株式会社 | Nucleic acid extraction method, cancer cell detection method and magnetic beads |
SG131016A1 (en) | 2005-09-19 | 2007-04-26 | Millipore Corp | Asymmetric porous adsorptive bead |
MX2008007716A (en) | 2005-12-13 | 2008-09-26 | Exthera Ab | Method for extracorporeal removal of a pathogenic microbe, an inflammatory cell or an inflammatory protein from blood. |
EP2015071A1 (en) * | 2007-07-13 | 2009-01-14 | FUJIFILM Corporation | Carrier, process for producing same, bioreactor, and chip for surface plasmon resonance analysis |
WO2009064977A2 (en) * | 2007-11-14 | 2009-05-22 | E.I. Du Pont De Nemours And Company | Dextran-based polymer tissue adhesive for medical use |
CA2723076A1 (en) * | 2008-05-09 | 2009-11-12 | Zhiping Liu | A molecule detecting system |
JP5253974B2 (en) * | 2008-11-14 | 2013-07-31 | 株式会社コーセー | MULTILAYER COATED PARTICLE, PROCESS FOR PRODUCING THE SAME, AND EXTERNAL SKIN CONTAINING THE SAME |
US20120149128A1 (en) * | 2009-02-23 | 2012-06-14 | Victor Manneh | Assays and assay devices |
EP2230515B1 (en) | 2009-03-16 | 2014-12-17 | Agilent Technologies, Inc. | Passivation of surfaces after ligand coupling |
US20120225496A1 (en) | 2009-11-17 | 2012-09-06 | Satoru Yoshida | Organic colored microparticles, diagnostic reagent kit containing the same, and in vitro diagnosis method |
CN106178161B (en) | 2009-12-01 | 2020-12-22 | 艾克塞拉医疗公司 | Method for removing cytokines from blood using surface immobilized polysaccharides |
CN102109521A (en) * | 2010-12-16 | 2011-06-29 | 中国环境科学研究院 | Immunolatex microsphere for detecting CpTI and preparation method thereof |
WO2012112724A1 (en) | 2011-02-15 | 2012-08-23 | Exthera Medical, Llc | Device and method for removal of blood-borne pathogens, toxins and inflammatory cytokines |
US8394647B2 (en) | 2011-02-17 | 2013-03-12 | Siemens Healthcare Diagnostics Inc. | Reducing non-covalently bound polysaccharide on supports |
EP2541250A1 (en) * | 2011-06-30 | 2013-01-02 | Koninklijke Philips Electronics N.V. | Molecular architecture on magnetic particles for affinity assays with low non-specific binding |
WO2013070653A1 (en) * | 2011-11-09 | 2013-05-16 | Board Of Trustees Michigan State University | Metallic nanoparticle synthesis with carbohydrate capping agent |
JP6226958B2 (en) * | 2012-04-18 | 2017-11-08 | シーメンス・ヘルスケア・ダイアグノスティックス・インコーポレーテッドSiemens Healthcare Diagnostics Inc. | COMPOUNDS AND METHODS FOR PRODUCING CONJUGATE REAGENTS |
EP2861273B1 (en) | 2012-06-13 | 2017-08-23 | ExThera Medical Corporation | Use of heparin and carbohydrates to treat cancer |
US9244083B2 (en) | 2012-11-30 | 2016-01-26 | Siemens Healthcare Diagnostics Inc. | Compositions and methods for detecting vitamin D |
US20140308751A1 (en) | 2013-04-12 | 2014-10-16 | Siemens Healthcare Diagnostics Inc. | Assays for Analyte Homologs |
EP3013445B1 (en) * | 2013-06-24 | 2019-11-06 | ExThera Medical Corporation | Blood filtration system containing mannose coated substrate |
US10124072B2 (en) * | 2013-09-18 | 2018-11-13 | Caliper Life Sciences, Inc. | In-vivo reactive species imaging |
WO2015069942A1 (en) | 2013-11-08 | 2015-05-14 | Exthera Medical Corporation | Methods for diagnosing infectious diseases using adsorption media |
BR112016024569B1 (en) | 2014-04-24 | 2023-01-03 | Exthera Medical Corporation | EX VIVO METHOD FOR REMOVING BACTERIA FROM A SPECIMEN TAKEN FROM AN INDIVIDUAL WHO IS SUSPECTED TO BE INFECTED WITH THE SAME |
JP6681349B2 (en) | 2014-06-27 | 2020-04-15 | シーメンス・ヘルスケア・ダイアグノスティックス・インコーポレーテッドSiemens Healthcare Diagnostics Inc. | Binding partners specific for vitamin D epimers |
KR20170016009A (en) | 2014-06-27 | 2017-02-10 | 지멘스 헬쓰케어 다이아그노스틱스 인크. | Binding partners specific for vitamin d epimers in vitamin d assays |
EP3197342B1 (en) | 2014-09-22 | 2020-08-05 | ExThera Medical Corporation | Wearable hemoperfusion device |
JP6852259B2 (en) * | 2016-01-07 | 2021-03-31 | 昭和電工マテリアルズ株式会社 | Separator and column |
US11911551B2 (en) | 2016-03-02 | 2024-02-27 | Exthera Medical Corporation | Method for treating drug intoxication |
EP3422943A4 (en) | 2016-03-02 | 2019-10-16 | ExThera Medical Corporation | Method for treating drug intoxication |
CN116337851A (en) * | 2018-07-18 | 2023-06-27 | 科美博阳诊断技术(上海)有限公司 | Homogeneous chemiluminescence detection kit and application thereof |
CN116559151A (en) * | 2018-07-18 | 2023-08-08 | 上海索昕生物科技有限公司 | Microsphere composition for chemiluminescence detection and application thereof |
CN110736737A (en) * | 2018-07-18 | 2020-01-31 | 博阳生物科技(上海)有限公司 | microsphere composition for chemiluminescence detection and application thereof |
US20210247398A1 (en) | 2018-07-30 | 2021-08-12 | Siemens Healthcare Diagnostics Inc. | Kits, microfluidics devices, and methods for performing biotin assays |
WO2020068541A1 (en) | 2018-09-25 | 2020-04-02 | Siemens Healthcare Diagnostics Inc. | Methods and compositions for removing biotin interference from assays using molecular traps |
CN116626285A (en) * | 2019-07-19 | 2023-08-22 | 科美博阳诊断技术(上海)有限公司 | Homogeneous chemiluminescence analysis method and application thereof |
CN116577512A (en) * | 2019-07-19 | 2023-08-11 | 科美博阳诊断技术(上海)有限公司 | Application of donor reagent in diagnosis of myocardial injury of subject |
CN116754757A (en) * | 2019-07-19 | 2023-09-15 | 上海索昕生物科技有限公司 | Donor particle for homogeneous chemiluminescence analysis and application thereof |
CN112240928B (en) * | 2019-07-19 | 2023-06-13 | 科美博阳诊断技术(上海)有限公司 | Homogeneous chemiluminescence analysis method and application thereof |
CN112240937B (en) * | 2019-07-19 | 2023-06-13 | 科美博阳诊断技术(上海)有限公司 | Application of donor reagent in diagnosis of bacterial inflammatory diseases of subject infection |
CN110441531B (en) * | 2019-08-17 | 2022-08-23 | 宁波奥丞生物科技有限公司 | Kit for detecting procalcitonin in blood and preparation method thereof |
CN110895283A (en) * | 2019-12-10 | 2020-03-20 | 宁波奥丞生物科技有限公司 | High-sensitivity D-dimer detection kit and use method thereof |
CN110907654A (en) * | 2019-12-10 | 2020-03-24 | 宁波奥丞生物科技有限公司 | Free estriol quantitative detection kit and preparation method thereof |
CN113125730B (en) * | 2019-12-31 | 2023-07-07 | 科美博阳诊断技术(上海)有限公司 | Homogeneous detection kit for interleukin 6 and application thereof |
CN113125711B (en) * | 2019-12-31 | 2023-07-28 | 科美博阳诊断技术(上海)有限公司 | Acceptor reagent and application thereof |
CN113125732B (en) * | 2019-12-31 | 2023-08-08 | 科美博阳诊断技术(上海)有限公司 | Homogeneous detection kit for interleukin 6 and application thereof |
CN113125721B (en) * | 2019-12-31 | 2023-07-07 | 科美博阳诊断技术(上海)有限公司 | Homogeneous detection kit for creatine kinase isozymes and application thereof |
CN113125714B (en) * | 2019-12-31 | 2023-06-16 | 科美博阳诊断技术(上海)有限公司 | Human immunodeficiency virus antibody detection kit and application thereof |
CN113125701B (en) * | 2019-12-31 | 2024-01-30 | 科美博阳诊断技术(上海)有限公司 | Homogeneous chemiluminescence detection kit and application thereof |
CN116400074A (en) * | 2019-12-31 | 2023-07-07 | 科美博阳诊断技术(上海)有限公司 | CRP detection kit and application thereof |
CN113125700B (en) * | 2019-12-31 | 2023-08-08 | 科美博阳诊断技术(上海)有限公司 | Homogeneous detection kit for creatine kinase isozymes and application thereof |
GB2616351A (en) * | 2021-12-01 | 2023-09-06 | Droplet Genomics Uab | Core-shell microcapsules, manufacturing processes and uses |
Family Cites Families (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3996345A (en) | 1974-08-12 | 1976-12-07 | Syva Company | Fluorescence quenching with immunological pairs in immunoassays |
CA1190838A (en) | 1981-07-17 | 1985-07-23 | Cavit Akin | Homogeneous nucleic acid hybridization diagnostics by non-radiative energy transfer |
EP0136347A1 (en) | 1983-02-25 | 1985-04-10 | Covalent Technology Corporation | Insoluble surfaces treated to inhibit non-specific protein binding |
US4891324A (en) | 1987-01-07 | 1990-01-02 | Syntex (U.S.A.) Inc. | Particle with luminescer for assays |
EP0438534A4 (en) | 1988-10-11 | 1991-09-11 | Coulter Corporation | Immunoreactant carriers having a novel biocompatible intermediate coating and process of making same |
US5466609A (en) * | 1990-10-31 | 1995-11-14 | Coulter Corporation | Biodegradable gelatin-aminodextran particle coatings of and processes for making same |
US5169754A (en) * | 1990-10-31 | 1992-12-08 | Coulter Corporation | Biodegradable particle coatings having a protein covalently immobilized by means of a crosslinking agent and processes for making same |
US5639620A (en) * | 1990-10-31 | 1997-06-17 | Coulter Corporation | Polymeric particles having a biodegradable gelatin or aminodextran coating and process for making same |
AU652804B2 (en) | 1991-01-19 | 1994-09-08 | Meito Sangyo Kabushiki Kaisha | Composition containing ultrafine particles of magnetic metal oxide |
FR2672128B1 (en) | 1991-01-28 | 1995-08-18 | Cis Bio Int | METHOD FOR MEASURING THE LUMINESCENCE EMITTED IN A LUMINESCENCE ASSAY. |
US5578498A (en) | 1991-05-22 | 1996-11-26 | Behringwerke Ag | Metal chelate containing compositions for use in chemiluminescent assays |
IL101945A (en) | 1991-05-22 | 1998-02-08 | Behringwerke Ag | Methods for determining an analyte using induced luminescence, and kits therefor |
DE4117782C2 (en) * | 1991-05-28 | 1997-07-17 | Diagnostikforschung Inst | Nanocrystalline magnetic iron oxide particles, processes for their production and diagnostic and / or therapeutic agents |
WO1994002486A1 (en) | 1992-07-20 | 1994-02-03 | Syntex (U.S.A.) Inc. | Novel chemiluminescent compounds and methods of use |
WO1994003501A1 (en) * | 1992-08-05 | 1994-02-17 | Meito Sangyo Kabushiki Kaisha | Small-diameter composite composed of water-soluble carboxypolysaccharide and magnetic iron oxide |
DE69331970T2 (en) | 1992-10-15 | 2002-12-19 | Coulter Int Corp | PARTICLES WITH GELATINE-AMINODEXTRAN COVERS AND METHOD FOR THE PRODUCTION THEREOF |
EP0716746B1 (en) | 1993-09-03 | 1999-03-17 | Behringwerke Ag | Fluorescent oxygen channeling immunoassays |
DE4428851C2 (en) | 1994-08-04 | 2000-05-04 | Diagnostikforschung Inst | Nanoparticles containing iron, their production and application in diagnostics and therapy |
DE19509694A1 (en) | 1995-03-08 | 1996-09-19 | Schering Ag | Use of magnetites to determine the perfusion of human tissue using MR diagnostics |
US5786161A (en) | 1996-06-06 | 1998-07-28 | Miltenyi Biotec. Gmbh | Isolation and characterization of allergen-binding cells for diagnosis of hypersensitivity |
US6231982B1 (en) | 1997-12-10 | 2001-05-15 | Dade Behring Inc. | Particle reagents having reduced matrix effects and containing an aldehyde-reactive functional group |
-
2000
- 2000-03-06 US US10/220,623 patent/US7179660B1/en not_active Expired - Lifetime
- 2000-03-06 WO PCT/US2000/005978 patent/WO2001067105A1/en active IP Right Grant
- 2000-03-06 EP EP00919371A patent/EP1264181B1/en not_active Expired - Lifetime
- 2000-03-06 CA CA2400993A patent/CA2400993C/en not_active Expired - Lifetime
- 2000-03-06 DE DE60035127T patent/DE60035127T2/en not_active Expired - Lifetime
- 2000-03-06 JP JP2001566027A patent/JP4448642B2/en not_active Expired - Lifetime
- 2000-03-06 ES ES00919371T patent/ES2287006T3/en not_active Expired - Lifetime
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113125705A (en) * | 2019-12-31 | 2021-07-16 | 博阳生物科技(上海)有限公司 | Homogeneous detection kit for myoglobin and application thereof |
CN113125703A (en) * | 2019-12-31 | 2021-07-16 | 博阳生物科技(上海)有限公司 | Homogeneous detection kit for myoglobin and application thereof |
CN113125703B (en) * | 2019-12-31 | 2023-08-04 | 科美诊断技术(苏州)有限公司 | Myoglobin homogeneous detection kit and application thereof |
CN113125705B (en) * | 2019-12-31 | 2023-08-04 | 科美诊断技术(苏州)有限公司 | Myoglobin homogeneous detection kit and application thereof |
Also Published As
Publication number | Publication date |
---|---|
JP2003526786A (en) | 2003-09-09 |
DE60035127T2 (en) | 2008-02-14 |
ES2287006T3 (en) | 2007-12-16 |
DE60035127D1 (en) | 2007-07-19 |
EP1264181A1 (en) | 2002-12-11 |
CA2400993C (en) | 2011-06-07 |
JP4448642B2 (en) | 2010-04-14 |
EP1264181B1 (en) | 2007-06-06 |
US7179660B1 (en) | 2007-02-20 |
WO2001067105A1 (en) | 2001-09-13 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA2400993A1 (en) | Carriers coated with polysaccharides, their preparation and use | |
JP2003526786A5 (en) | ||
US9738745B2 (en) | Particles containing multi-block polymers | |
US5283079A (en) | Process to make magnetically responsive fluorescent polymer particles | |
US6013531A (en) | Method to use fluorescent magnetic polymer particles as markers in an immunoassay | |
CA1255216A (en) | Immunoassay for the detection of ligands | |
US4278651A (en) | Supported receptor and use thereof in an assay | |
AU634631B2 (en) | Magnetically responsive fluorescent polymer particles and application thereof | |
EP0232816B1 (en) | Heterogeneous specific binding assay employing an aggregatable binding reagent | |
US5795719A (en) | Biotinylated latex microsphere, process for the preparation of such a microsphere and use as agent for biological detection | |
Margel et al. | Polyacrolein microspheres as a new tool in cell biology | |
JP2000516345A (en) | Multiple flow immunoassay using magnetic particles as solid phase | |
US6074884A (en) | Stable protein-nickel particles and methods of production and use thereof | |
JPH0258590B2 (en) | ||
JPS59166866A (en) | Analysis method | |
MY100973A (en) | Immuno- agglutination suspensions | |
US5397695A (en) | Attachment of compounds to polymeric particles using carbamoylonium compounds and a kit containing same | |
US4108975A (en) | Radioimmunoassay system | |
TW200426369A (en) | Reduction of the hook effect in assay devices | |
JP3192149B2 (en) | Magnetic particles having gelatin and immunoassay using the same | |
GB2221466A (en) | Biologically reactive particles with biological, therapeutic and chromatographic applications | |
GB2123146A (en) | Dual parameter flow immunoassays | |
Fairman et al. | Unique morphology of HeLa cell attachment, spreading and detachment from microcarrier beads covalently coated with a specific and non-specific substratum | |
JPH07151759A (en) | Reagent for acquiring reactant, intermediate thereof and acquiring method | |
Margel | Polyaldehyde microspheres as probes for cell membranes |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
EEER | Examination request | ||
MKEX | Expiry |
Effective date: 20200306 |